← Back to catalogue
TAPESTRY RC Biointegrative Implant System
FDA UDIClass II (US FDA UDI)
by Embody, Inc.
Identity
- Trade Name
- TAPESTRY RC Biointegrative Implant System FDA UDI
- Generic Name
- Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI
- Device Name
- Convenience Kit FDA UDI
- Model / Reference
- TR-2626-M6 FDA UDI
- Description
- Convenience Kit FDA UDI
Identifiers
- Catalog Number
- TR-2626-M6 FDA UDI
- Primary DI / UDI-DI
- 00810063820527 FDA UDI
- FDA Product Code
- OWY FDA UDIMAI FDA UDIGEA FDA UDI
- GMDN Term
- Arthroscopic surgical procedure kit, non-medicated, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.3300 FDA UDI888.3030 FDA UDI878.4800 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Safe FDA UDI
TAPESTRY RC Biointegrative Implant System by Embody, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Embody, Inc.
Sources (1)
- FDA UDI edd69de2-6c09-466e-aa5e-936aca2f4334 35 fields · synced Jun 8, 2026